The University of Texas MD Anderson Cancer Center and Myriad Genetics, Inc. have announced a five-year strategic alliance to advance the clinical evaluation of Myriad’s molecular residual disease (MRD) assay, Precise MRD. This collaboration leverages Myriad’s expertise in oncology diagnostics and MD Anderson’s leadership in clinical and translational research to assess the test’s validity and utility.
“We look forward to working with MD Anderson to evaluate Precise MRD’s role in cancer care,” said Dale Muzzey, PhD, Chief Scientific Officer at Myriad Genetics. “Our studies will explore how this ultrasensitive test can refine treatment strategies and improve patient outcomes. By detecting tumor-derived DNA at significantly lower levels than first-generation MRD tests, Precise MRD has the potential to enhance therapy-response and recurrence monitoring.”
MD Anderson and Myriad will conduct retrospective and prospective studies across breast, gastrointestinal, genitourinary, and gynecologic cancers to generate evidence supporting national guideline inclusion and provider adoption. MD Anderson investigators will lead patient enrollment, sample collection, data analysis, and manuscript development, while Myriad will provide funding, MRD testing, and scientific research support, including potential milestone and royalty payments.
“This collaboration integrates Myriad’s cutting-edge MRD technology with MD Anderson’s disease-focused expertise,” said Christopher Flowers, M.D., division head of Cancer Medicine at MD Anderson. “We aim to explore MRD’s role in relapse monitoring, risk stratification, and potential intervention strategies.”
The alliance builds on existing collaborations in breast cancer and renal cell carcinoma, further expanding research efforts to enhance cancer care.